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FREQUENCIES OF PLATELET-SPECIFIC ALLOANTIGEN SYSTEMS 1–5 IN THREE DISTINCT ETHNIC GROUPS IN BRAZIL
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State University of Campinas. Hematology and Hemotherapy Center. Campinas, SP, Brasil
State University of Campinas. Hematology and Hemotherapy Center. Campinas, SP, Brasil
State University of Campinas. Hematology and Hemotherapy Center. Campinas, SP, Brasil
Evandro Chagas Institute. Belém, PA, Brasil
Evandro Chagas Institute. Belém, PA, Brasil
Universidade Federal da Bahia. Salvador, BA, Brasil
State University of Campinas. Hematology and Hemotherapy Center. Campinas, SP, Brasil
State University of Campinas. Hematology and Hemotherapy Center. Campinas, SP, Brasil
State University of Campinas. Hematology and Hemotherapy Center. Campinas, SP, Brasil
State University of Campinas. Hematology and Hemotherapy Center. Campinas, SP, Brasil
Evandro Chagas Institute. Belém, PA, Brasil
Evandro Chagas Institute. Belém, PA, Brasil
Universidade Federal da Bahia. Salvador, BA, Brasil
State University of Campinas. Hematology and Hemotherapy Center. Campinas, SP, Brasil
State University of Campinas. Hematology and Hemotherapy Center. Campinas, SP, Brasil
Abstract
The human platelet antigen (HPA) systems are related to
immune platelet disorders as well as to the development
of occlusive vascular disease. Several distinct biallelic
HPA systems are known, and a heterogeneous distribution
of HPA alleles has been described among distinct
ethnic groups. In this study we genotyped 320 carefully
selected individuals from three distinct ethnic groups in
Brazil (Caucasians, Blacks and Amazonian Indians) for
the HPA-1, -2, -3, -4 and -5 systems. A similar prevalence
for all HPA alleles was found in Brazilians of Caucasian
and Black descent. These data contrast with those
reported for similar ethnic groups in other countries.
Among the Amazonian Indians, no b allele of the HPA-
1, -4 and -5 systems was identified. The data presented
here could be useful in the diagnosis of alloimmune
platelet disease, in genetic counselling and in the development
of screening programmes for HPA-related diseases
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